FDA UDI In Commercial Distribution 🇺🇸 United States

HALYARD

DI: 10680651200805 · Model: SGL96080 · Ansell
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
HALYARD
Primary DI
10680651200805
Version / Model
SGL96080
Catalog Number
SGL96080
Company Name
Ansell
Labeler DUNS
120522524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-12
Public Version
1
Public Version Date
2024-07-22
Public Version Status
New
Public Device Record Key
1a05497b-7894-4569-aa88-39c12c8c523e

Device Description

HALYARD SGL96080 Polyisoprene Textured Size (8.0), Powder-Free Polyisoprene Surgical Glove

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KGO Surgeon'S Gloves

GMDN Terms

Code Name
56293 Polyisoprene surgical glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 20680651200802
Primary 10680651200805
Package 30680651200809

Customer Contacts

Phone
775-470-7106
Phone
775-746-6600

Device Sizes

Type Value Unit Text
Device Size Text, specify 8.0